Neural Mechanisms Underlying the Antidepressant Effects of Sleep Deprivation



Status:Recruiting
Conditions:Depression, Insomnia Sleep Studies
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:21 - 50
Updated:9/5/2018
Start Date:April 1, 2016
End Date:January 31, 2020
Contact:Holly Barilla
Email:holly.barilla@uphs.upenn.edu
Phone:215-746-4384

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From 40 to 60% of patients with depression experience a rapid and significant improvement of
mood with one night of sleep deprivation (SD). The neural mechanisms underlying this effect
have not been elucidated. Recent advances in functional neuroimaging have provided new
opportunities to investigate state changes in regional brain function, along with a better
understanding of the neural networks affected by depression and SD. Here we propose to study
a group of N=48 antidepressant-free male and female patients with current depression symptom
and N=12 healthy controls with no history of mood disorders before and after SD to provide
mechanistic insight into the neural substrates underlying the antidepressant effects of SD.
We hypothesize that SD-induced concurrent functional activity and connectivity changes in
multiple brain networks related to different depressive symptom dimensions including emotion
regulation, attention, arousal, self-referential, and reward processing will underlie the
rapid and transient antidepressant effects of SD. Using an ABA design, multimodal brain
imaging along with more traditional electroencephalographic (EEG) and neurobehavioral testing
data will be acquired at baseline after normal sleep, during one night of total SD, and after
one night of recovery sleep using a 5-day in laboratory protocol during which subjects will
be continuously monitored by trained staff.


Inclusion Criteria:

- Current depression as assessed on the HDRS-17 (for depressed group only)

- Body mass index within 15% of normal

- Stable, normally-timed sleep-wake cycle defined by: a. Habitual nocturnal sleep
duration between 6h and 9h. b. Habitual morning awakening between 0600h and 0800h.

- Able to comprehend English, as all questionnaires are in this language

- Ability to provide informed consent

Exclusion Criteria:

- Shift work, transmeridian travel or irregular sleep/wake routine in past 60 days

- A sleep disorder other than insomnia

- History of bipolar disorder, delirium, dementia, amnestic disorder, schizophrenia and
other psychotic disorders

- No history of depression for the control group.

- Alcohol or drug abuse in the past year

- A current smoker.

- Any acute or chronic, debilitating medical conditions, epilepsy, or thyroid disease.

- Metallic implants, pacemakers or tattoos, or history of working in metal workshops.

- Claustrophobic, or intolerant of the scanner environment.

- For women, pregnancy will exclude participation.
We found this trial at
1
site
3451 Walnut St
Philadelphia, Pennsylvania 19104
1 (215) 898-5000
Phone: 215-746-4384
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